✨ AI Summary
The Quality Control Analyst will be responsible for analyzing finished products and bulk samples, performing chemical and physical analysis according to methods and specifications. Key duties include preparing chemical reagents, using pharmacopeias, writing analytical reports and COAs, preparing working standards, and documenting analytical results. The role also involves retesting raw materials and analyzing solid dosage forms, while complying with GLP and procedures.
Requirements
Bachelor's Degree of Pharmaceutical Sciences or ChemistrySciences.2-4 years of proven experience in raw material analysis.Good experience in handling of HPLC & GC &Atomic.Professional using Computer & Microsoft Office.Organized and detail-oriented.Good communication skills.Analytical skills - Active learning.
Description
Analyzing finished products and their bulk samples (Performing dissolution profile will be an advance).Able to perform on different lab instruments (Agilent and Shimadzu HPLC will be an advance).Prepare different chemical reagents used in routine analysis.Using different pharmacopeias.Writing the Analytical Reports and COA.Chemical and physical analysis according to method and specification after having the necessary training.Preparation of working standard.Intermediate check for equipment concerns in the raw material lab.Preparation of chemical reagents and other required volumetric solutions as directed.Documentation of analytical results according to the predetermined procedure.Reporting deviations, suspect results, out-of-specification results, and any other required reports.Retest of raw materials.Analysis of Solid dosage formsComplying with the applicable GLP and procedures after having the necessary training